Exploring low cost, highly active, and durable electrocatalysts for oxygen evolution reaction (OER) is of prime importance to boost energy conversion efficiency. Perovskite fluorides are emerging as alternative electrocatalysts for OER, however, their intrinsically active sites during real operation are still elusive. Herein, the self-reconstruction on newly designed NiFe coupled perovskite fluorides during OER process is demonstrated. In situ Raman spectroscopy, ex situ X-ray absorption spectroscopy, and theoretical calculation reveal that Fe incorporation can significantly activate the self-reconstruction of perovskite fluorides and efficiently lower the energy barrier of OER. Benefiting from self-reconstruction and low energy barrier, the KNi Fe F @nickel foam (KNFF2@NF) electrocatalyst delivers an ultralow overpotential of 258 mV to afford 100 mA cm and an excellent durability for 100 h, favorably rivaling most the state-of-the-art OER electrocatalysts. This protocol provides the fundamental understanding on OER mechanism associated with surface reconstruction for perovskite fluorides.
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http://dx.doi.org/10.1002/advs.202201916 | DOI Listing |
ACS Nano
January 2025
College of Materials and Chemistry & Chemical Engineering, Nuclear Technology Key Laboratory of Earth Science, Chengdu University of Technology, Chengdu 610059, China.
The precise patterning of elastic semiconductors holds encouraging prospects for unlocking functionalities and broadening the scope of optoelectronic applications. Here, perovskite films with notable elasticity capable of stretching over 250% are successfully fabricated by using a continuous-wave (CW) laser-patterning technique. Under CW laser irradiation, perovskite nanoparticles (NPs) undergo meticulous crystallization within the thermoplastic polyurethane (TPU) matrix, which yields the capability of an unparalleled stretch behavior.
View Article and Find Full Text PDFChem Sci
December 2024
Tianjin Key Laboratory of Functional Crystal Materials, Institute of Functional Crystal, College of Materials Science and Engineering, Tianjin University of Technology Tianjin 300384 China
Non-centrosymmetric (NCS) compounds can exhibit many symmetry-dependent functional properties, yet their rational structure design remains a great challenge. Herein, a strategy to introduce F-centered octahedra to construct a perovskite-type framework filled by π-conjugated [BO] dimers is proposed to obtain NCS compounds. The first examples of antiperovskite or double antiperovskite borate fluorides, [(M/Ba)Ca]F[BO] (M = K, Rb) and [CsBaCa]F[BO], have been successfully designed and synthesized.
View Article and Find Full Text PDFSmall
December 2024
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, Shaanxi Key Laboratory for Advanced Energy Devices, Shaanxi Engineering Lab for Advanced Energy Technology, School of Materials Science and Engineering, Shaanxi Normal University, Xi'an, 710119, P. R. China.
Mechanistic understanding of how electrode-electrolyte interfaces evolve dynamically is crucial for advancing water-electrolysis technology, especially the restructuring of catalyst surface during complex electrocatalytic reactions. However, for perovskite fluorides, the mechanistic exploration for the influence of the dynamic restructuring on their chemical property and catalytic mechanism is unclear due to their poor conductivity that makes the definition of electrocatalyst structure difficult. Herein, for oxygen evolution reaction (OER), various operando characterizations are employed to investigate the structure-activity relationships of the KNiFe F@NF.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
College of Chemistry and Environmental Science, Inner Mongolia Normal University, Hohhot 010022, China. Electronic address:
Electrochemical production of NH from NO offers a solution to the environmental issue of excess NO but is challenged by the lack of efficient, sensitive electrocatalysts with high NH yield rate and Faraday efficiency (FE). Herein, a medium-entropy perovskite fluoride (KMF, M = Co/Ni/Fe/Ti) was prepared as efficient electrocatalysts to produce NH via the NO reduction reaction (NORR). By introducing various transition metals at the M-sites, the charge distribution at the M-site octahedral units was adjusted to increase the disorder of KMF, resulting in an optimized electronic structure with high intrinsic NORR performance.
View Article and Find Full Text PDFMater Horiz
December 2024
Quantum Materials and Devices Unit, Institute of Nano Science and Technology, Knowledge City, Sector 81, Mohali 140306, India.
The 'pyro-phototronic effect' plays a nontrivial role in advancing ferroelectric (FE) devices of light detectors, light-emitting diodes, and other smart technologies. In this work, a premier FE copolymer, poly(vinylidene fluoride--trifluoro ethylene) (P(VDF-TrFE)), is reinforced with a lead-free double perovskite, CsSnI, to render profound properties in a hybrid nanostructure. It presents a unique example of the coupling of ferro-, pyro- and piezo-electrics to the 'photoexcitation' of exotic charges that actively empower the synergetic features.
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